Cargando…

Single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins

Protein oligomerization is central to biological function and regulation, yet its experimental quantification and measurement of dynamic transitions in solution remain challenging. Here, we show that single molecule mass photometry quantifies affinity and polydispersity of heterogeneous protein comp...

Descripción completa

Detalles Bibliográficos
Autores principales: Liebthal, Michael, Kushwah, Manish Singh, Kukura, Philipp, Dietz, Karl-Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571717/
https://www.ncbi.nlm.nih.gov/pubmed/34765909
http://dx.doi.org/10.1016/j.isci.2021.103258
_version_ 1784595083526406144
author Liebthal, Michael
Kushwah, Manish Singh
Kukura, Philipp
Dietz, Karl-Josef
author_facet Liebthal, Michael
Kushwah, Manish Singh
Kukura, Philipp
Dietz, Karl-Josef
author_sort Liebthal, Michael
collection PubMed
description Protein oligomerization is central to biological function and regulation, yet its experimental quantification and measurement of dynamic transitions in solution remain challenging. Here, we show that single molecule mass photometry quantifies affinity and polydispersity of heterogeneous protein complexes in solution. We demonstrate these capabilities by studying the functionally relevant oligomeric equilibria of 2-cysteine peroxiredoxins (2CPs). Comparison of the polydispersity of plant and human 2CPs as a function of concentration and redox state revealed features conserved among all 2CPs. In addition, we also find species-specific differences in oligomeric transitions, the occurrence of intermediates and the formation of high molecular weight complexes, which are associated with chaperone activity or act as a storage pool for more efficient dimers outlining the functional differentiation of human 2CPs. Our results point to a diversified functionality of oligomerization for 2CPs and illustrate the power of mass photometry for characterizing heterogeneous oligomeric protein distributions in near native conditions.
format Online
Article
Text
id pubmed-8571717
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-85717172021-11-10 Single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins Liebthal, Michael Kushwah, Manish Singh Kukura, Philipp Dietz, Karl-Josef iScience Article Protein oligomerization is central to biological function and regulation, yet its experimental quantification and measurement of dynamic transitions in solution remain challenging. Here, we show that single molecule mass photometry quantifies affinity and polydispersity of heterogeneous protein complexes in solution. We demonstrate these capabilities by studying the functionally relevant oligomeric equilibria of 2-cysteine peroxiredoxins (2CPs). Comparison of the polydispersity of plant and human 2CPs as a function of concentration and redox state revealed features conserved among all 2CPs. In addition, we also find species-specific differences in oligomeric transitions, the occurrence of intermediates and the formation of high molecular weight complexes, which are associated with chaperone activity or act as a storage pool for more efficient dimers outlining the functional differentiation of human 2CPs. Our results point to a diversified functionality of oligomerization for 2CPs and illustrate the power of mass photometry for characterizing heterogeneous oligomeric protein distributions in near native conditions. Elsevier 2021-10-13 /pmc/articles/PMC8571717/ /pubmed/34765909 http://dx.doi.org/10.1016/j.isci.2021.103258 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liebthal, Michael
Kushwah, Manish Singh
Kukura, Philipp
Dietz, Karl-Josef
Single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins
title Single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins
title_full Single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins
title_fullStr Single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins
title_full_unstemmed Single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins
title_short Single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins
title_sort single molecule mass photometry reveals the dynamic oligomerization of human and plant peroxiredoxins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571717/
https://www.ncbi.nlm.nih.gov/pubmed/34765909
http://dx.doi.org/10.1016/j.isci.2021.103258
work_keys_str_mv AT liebthalmichael singlemoleculemassphotometryrevealsthedynamicoligomerizationofhumanandplantperoxiredoxins
AT kushwahmanishsingh singlemoleculemassphotometryrevealsthedynamicoligomerizationofhumanandplantperoxiredoxins
AT kukuraphilipp singlemoleculemassphotometryrevealsthedynamicoligomerizationofhumanandplantperoxiredoxins
AT dietzkarljosef singlemoleculemassphotometryrevealsthedynamicoligomerizationofhumanandplantperoxiredoxins